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OSCILLOGEL SIGNED

An enzyme-based self-oscillating gel

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 OSCILLOGEL project word cloud

Explore the words cloud of the OSCILLOGEL project. It provides you a very rough idea of what is the project "OSCILLOGEL" about.

regulatory    chemoresponsive    rigid    reaction    responsive    oscillation    power    mostly    biochemical    self    popular    oscillatory    unreacted    drive    itself    property    valve    environment    biologically    arise    urease    subsystems    synthetic    linked    morphogenesis    understand    feedback    mechano    swells    components    diffusion    biocompatible    closing    collective    off    lowers    merely    mechanical    motility    oscillator    pull    periodicity    elasticity    versa    operated    stress    found    clue    eliminated    living    though    big    shrinks    biological    load    fit    engineer    release    gel    urea    inconvenience    continual    hydrogel    wish    biochemistry    material    enzyme    reactions    counterintuitive    interdependence    emerges    underlying    external    lacks    immobilized    lacking    inorganic    energy    transport    functions    motion    force    first    forwards    dynamic    generally    flow    uniform    models    individually    autonomous    constant    vice    reactants    intrinsic    attributed    stimuli    coupled    corresponding    chemical    source    mechanics    obtain    loops    exploring    insufficiently    fresh    chemistry    opening    structural    maintained    differentiation    lifts    continuous    periodic   

Project "OSCILLOGEL" data sheet

The following table provides information about the project.

Coordinator
THE UNIVERSITY OF SHEFFIELD 

Organization address
address: FIRTH COURT WESTERN BANK
city: SHEFFIELD
postcode: S10 2TN
website: www.shef.ac.uk

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country United Kingdom [UK]
 Total cost 183˙454 €
 EC max contribution 183˙454 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2017
 Funding Scheme MSCA-IF-EF-CAR
 Starting year 2019
 Duration (year-month-day) from 2019-02-01   to  2021-01-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    THE UNIVERSITY OF SHEFFIELD UK (SHEFFIELD) coordinator 183˙454.00

Map

 Project objective

Self-oscillation is a periodic motion generated and maintained by a source of power that lacks the corresponding periodicity. In living systems several periodic motility processes or structural differentiation arise with no on-off stimuli, merely under the continual flow-in and flow-out of material and energy. The popular synthetic dynamic models use oscillatory chemical reactions to drive the system, though in most real cases no underlying biochemical oscillator is found. One clue is in the interdependence of chemistry and mechanics (stress, elasticity, or transport). Periodicity is counterintuitive because it cannot be attributed to any of the subsystems individually: this property emerges only through the collective behaviour of the components, as a systems-level property. To understand biological systems, we need to understand how these properties and functions are generated and controlled. Feedback-loops between chemical and mechanical processes are intrinsic in morphogenesis, though mechano-chemical feedback is generally still lacking in synthetic systems. I build coupled reaction-diffusion-mechanics systems, where a chemoresponsive hydrogel swells and shrinks (and, e.g., lifts and lowers a load) in a constant and uniform unreacted chemical environment, with no external stimuli. The chemistry is not oscillatory in itself, that is, if the gel is rigid or insufficiently responsive. Previous systems (mostly with inorganic reactions) operated under the continuous flow of fresh reactants. This inconvenience would be eliminated by making a big step forwards to biochemistry, where the reaction is linked to an enzyme immobilized in the gel. First we wish to demonstrate such a biocompatible system with the urease-urea reaction. After exploring the operating conditions, this autonomous system could fit to engineer regulatory functions by opening-closing a valve or to obtain biologically meaningful chemical responses by applying a force (pull, release) and vice versa.

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